Systems and methods for improved connection to wound dressings in conjunction with reduced pressure wound treatment systems

ABSTRACT

A system for applying reduced pressure to tissue includes a multi-lumen reduced pressure delivery tube having a proximate end, a distal end, a primary lumen extending through the conduit from the proximate end to the distal end, and an ancillary lumen extending through the conduit from the proximate end to the distal end. A vacuum pump is coupled to the proximate end of the primary lumen, and a reduced pressure adapter is coupled to the distal end of the reduced pressure delivery tube. The adapter includes channels to direct liquid away from the ancillary lumens and into the primary lumen.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. patent applicationSer. No. 15/247,566, filed Aug. 25, 2016, which is a divisionalapplication of U.S. patent application Ser. No. 14/579,664, filed Dec.22, 2014, now U.S. Pat. No. 9,452,246, which is a continuationapplication of U.S. patent application Ser. No. 13/651,284, filed Oct.12, 2012, now U.S. Pat. No. 8,951,236, which is a divisional applicationof U.S. patent application Ser. No. 12/650,316, filed Dec. 30, 2009, nowU.S. Pat. No. 8,308,703, which is a divisional application of U.S.patent application Ser. No. 11/702,822, filed Feb. 6, 2007, now U.S.Pat. No. 7,651,484, which claims the benefit of U.S. ProvisionalApplication No. 60/765,548, filed Feb. 6, 2006, all of which are herebyincorporated by reference.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The present invention relates to generally to systems and methods forproviding reduced pressure treatment to tissue, particularly openwounds. The present invention relates more specifically to systems andmethods for improving the connection between a tissue dressing andreduced pressure source instrumentation used in conjunction with reducedpressure wound treatment (RPWT).

2. Description of the Related Art

Various therapies have been developed over time to facilitate theprocess of wound closure and healing. Wound closure generally involvesthe inward migration of epithelial and subcutaneous tissue adjacent thewound. This migration is ordinarily assisted by the inflammatoryprocess, whereby blood flow is increased and various functional celltypes are activated. As a result of the inflammatory process, blood flowthrough damaged or broken vessels is stopped by capillary levelocclusion, whereafter cleanup and rebuilding operations may begin.Unfortunately, this process is hampered when a wound is large or hasbecome infected. In such wounds, a zone of stasis (i.e. an area in whichlocalized swelling of tissue restricts the flow of blood to the tissues)forms near the surface of the wound.

Without sufficient blood flow, the epithelial and subcutaneous tissuessurrounding the wound not only receive diminished oxygen and nutrients,but are also less able to successfully fight bacterial infection and,thus, less able to naturally close the wound. Additionally, some woundsharden and inflame to such a degree that closure by stapling or suturingis not feasible. Examples of wounds not readily treatable with staplesor suturing include large, deep, open wounds; decubitus ulcers; ulcersresulting from chronic osteomyelitis; and partial thickness burns thatsubsequently develop into full thickness burns.

As a result of the shortcomings of mechanical wound closure devices,methods and apparatus for draining wounds by applying continuous and/orperiodic reduced pressures have been developed. When applied over asufficient area of the wound, such reduced pressures have been found topromote the migration of epithelial and subcutaneous tissues toward thewound. In practice, the application to a wound of reduced pressuretypically involves the mechanical-like contraction of the wound withsimultaneous removal of excess fluid. In this manner, RPWT augments thebody's natural inflammatory process while alleviating many of the knownintrinsic side effects, such as the production of edema caused byincreased blood flow absent the necessary vascular structure for propervenous return.

Vacuum or reduced pressure induced healing of open wounds has recentlybeen popularized by Kinetic Concepts, Inc. of San Antonio, Tex., throughits commercially available RPWT systems product line. The reducedpressure induced healing process has been described in commonly assignedU.S. Pat. No. 4,969,880, issued on Nov. 13, 1990 to Zamierowski, as wellas in its related patents, including U.S. Pat. No. 5,100,396, issued onMar. 31, 1992; U.S. Pat. No. 5,261,893, issued on Nov. 16, 1993; andU.S. Pat. No. 5,527,293 issued Jun. 18, 1996, the disclosures of whichare each incorporated herein by reference. Further improvements andmodifications of the RPWT process are also described in U.S. Pat. No.6,071,267, issued on Jun. 6, 2000 to Zamierowski and U.S. Pat. Nos.5,636,643 and 5,645,081 issued to Argenta et al. on Jun. 10, 1997 andJul. 8, 1997 respectively, the disclosures of which are eachincorporated by reference as though fully set forth herein. Additionalimprovements have also been described in U.S. Pat. No. 6,142,982, issuedon May 13, 1998 to Hunt, et al.

One important component of a RPWT system is the device or structure thatconnects the reduced pressure source (a vacuum pump, typically) to thecomponents (a granular foam layer, typically) enclosed within the pad orwound dressing. This reduced pressure port structure must adhere to thewound dressing and be in fluid communication with the foam layer of thedressing. The port is preferably of low profile, in the nature of anattachment pad, in order to provide both comfort and safety to thepatient. Various efforts have been made in the past to provide suitableadapter configurations to effectively connect the reduced pressuresource (through tubing, typically) to a tissue site.

Commensurate with the application of continuous and/or periodic reducedpressures to a wound is a coordinated monitoring of the pressure presentat the tissue site as a result of the application of the RPWT system. Ithas become important, therefore, to provide systems that are capable ofmonitoring and responding to changes in the level of reduced pressureapplied at the tissue site. Various regimens of RPWT that involvecycling the reduced pressure applied to the wound have been found to bebeneficial under certain circumstances. Other situations benefit from aconstant but closely regulated application of reduced pressure. In anycase, it becomes valuable to accurately monitor the level of reducedpressure applied at the tissue site.

Generally it is not possible to characterize the pressure level at thetissue site by simply measuring the level of reduced pressure that thereduced pressure source is providing, either at the source or in theconduit lines connecting the source to the wound dressing. Fluid flowwithin the primary lumen of tubing associated with RPWT systems preventsusing pressure level measurements at the instrumentation from beingaccurate indicators of the level or stability of the pressure at thetissue site itself. Other methods for directly monitoring the woundpressure levels are therefore required.

Some efforts have been made in the past to provide a separate pressuresensing or measurement conduit to the wound site connected to monitoringinstrumentation. These efforts have typically provided a separate lumenwithin the RPWT tubing or have utilized a separate section of tubingaltogether. The assumption being made with such systems, however, isthat the ancillary measurement lumen or measurement tube is open andclear down to its port at the wound dressing. This is not always a validassumption as, despite the fact that the measurement lumen is notforcibly drawing fluids in as is being done in the primary flow lumen ofthe RPWT system, it still collects fluids and other materials thatinhibit or altogether block its function. The typically smallercross-section of such measurement lumens may reduce the port size, andtherefore the chance of fluid or other matter entering the port, but thesame smaller cross-section results in even minor blockages becomingsignificant.

SUMMARY OF THE INVENTION

Exemplary embodiments of the present invention provide improvements tothe structure and use of the connector elements between the wounddressing and the reduced pressure source in a reduced pressure woundtreatment (RPWT) system. More specifically certain exemplary embodimentsprovide:

(A) A low profile reduced pressure adapter that improves the reliabilityof operation and prevents or reduces instances of unintentional fluidingress into measurement lumens;

(B) An improved reduced pressure delivery tube comprising an oval tubingstructure with a larger inner lumen and smaller outer lumens forsupporting the dynamic pressure functionality described below;

(C) An improved and dynamic method of measuring wound pressure thatovercomes certain problems with existing pressure control in RPWTsystems;

(D) An improved reduced pressure adapter structure having rotationalfunctionality to facilitate the comfort of the attachment to thepatient; and

(E) A structure to provide indications of the presence of bacteriawithin the reduced pressure adapter and fluids transported therethrough.

The improved reduced pressure adapter includes a conduit housing with aprimary conduit and at least one secondary conduit for fluid connectionto a wound dressing. The reduced pressure adapter also may include abase with a substantially circular shape. The conduit housing includes arecessed region defining an entry surface. The primary conduit connectsthe entry surface to a primary lumen of a multi-lumen reduced pressuredelivery tube, and ancillary conduits connect the entry surface toancillary lumens of the multi-lumen reduced pressure delivery tube.Channels positioned on the entry surface preferentially route liquidsand other fluids into the primary conduit in order to prevent theclogging of the ancillary conduits, which are generally utilized tomeasure pressure within the wound dressing.

The improved reduced pressure delivery tube incorporates a largerprimary inner lumen to effect the conduction of reduced pressure to thetissue and fluids away from the tissue. Smaller outer ancillary lumensare provided to support the hereinafter described dynamic pressurefunctionality that insures the continuity of accurate pressuremeasurements through the monitoring of the open or closed (clogged)state of each of the ancillary lumens. The reduced pressure deliverytube may be mated to the improved reduced pressure adapter describedabove, or may be used with other adapters to fluidly connect a reducedpressure source and pressure sensors to a porous pad or otherdistribution manifold.

The improved method of measuring pressure addresses certain problemswith existing pressure control in RPWT systems that result fromexcessive fluid incursion into the measurement lumens of the system.Each of the ancillary lumens are monitored for their responsiveness tochanges in the reduced pressure source (and thus in the wound dressingitself). A slow response in one of the ancillary lumens is indicative ofclogging in that lumen, and as a result, the RPWT system considers thepressure measurement from the clear ancillary lumen as the accuratemeasurement. The system further allows for the introduction of elevatedpressure into the clogged lumen in a manner that may serve to clear thelumen of fluid obstruction, all the while the second of the twoancillary lumens may continue to function as a monitoring channel formeasuring the pressure at the tissue site.

In other embodiments the improved reduced pressure adapter structureincorporates rotational functionality to improve the patient'sconvenience and comfort. The conduit housing is positioned on androtatably attached to the perimeter base in a manner that allows thereduced pressure adapter and attached tubing to rotate with respect tothe wound dressing thereby reducing strain on the dressing and thereduced pressure adapter.

Finally, in yet further embodiments, the improved reduced pressureadapter incorporates an internal surface, preferably formed on theinterior perimeter wall of the conduit housing of the adapter, toprovide indications of the presence of bacteria within the adapterenclosure and therefore the fluids transported through the adapter. Thisindicator surface retains a layer of material sensitive to the volatileorganic compounds (VOC) associated with various targeted microorganisms.The VOC sensitive surface develops a specific color pattern depending onthe type of VOC and therefore the type of microorganism present. Thecolor pattern may be visually discerned through the clear material ofthe reduced pressure adapter construction or may be automaticallydetected by photometric color analysis using one of a variety of suchphotometric sensor devices.

Finally, many other features, objects, and advantages of the presentinvention will be apparent to those of ordinary skill in the relevantarts, especially in light of the foregoing discussions and the followingdrawings and exemplary detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

Although the scope of the present invention is much broader than anyparticular embodiment, a detailed description of the preferredembodiment follows, together with illustrative figures, wherein likereference numerals refer to like components, and wherein:

FIG. 1 is a partially schematic, perspective view of the generalarrangement of the components of a reduced pressure wound treatment(RPWT) system incorporating the improved elements of an exemplaryembodiment of the present invention;

FIG. 2 is a perspective view of the underside (open side) of an improvedreduced pressure adapter according to an embodiment of the presentinvention;

FIG. 3 is a plan view of the topside (closed side) of the improvedreduced pressure adapter of FIG. 2;

FIG. 4 is a first side view of the improved reduced pressure adapter ofFIG. 2;

FIG. 5 is an end view of the improved reduced pressure adapter of FIG.2;

FIG. 6 is a second side view of the improved reduced pressure adapter ofFIG. 2;

FIG. 7 is a plan view of the underside (open side) of the improvedreduced pressure adapter of FIG. 2, the underside configured accordingto a first exemplary embodiment of the present invention;

FIG. 8 is a plan view of the underside (open side) of the improvedreduced pressure adapter of FIG. 2, the underside configured accordingto another exemplary embodiment of the present invention;

FIG. 9 is a detailed view of a recessed region of the reduced pressureadapter of FIGS. 7 and 8;

FIG. 10 is a perspective view of an open end of an improved reducedpressure delivery tube according to an exemplary embodiment of thepresent invention;

FIG. 11 is a longitudinal cross-sectional view of the improved reducedpressure delivery tube of FIG. 10;

FIG. 12 is a schematic block diagram illustrating the arrangement andfunctionality of a reduced pressure system according to an exemplaryembodiment of the present invention;

FIG. 13 is an exploded perspective view of an improved reduced pressureadapter according to an exemplary embodiment of the present invention,the reduced pressure adapter incorporating elements that providerotational functionality;

FIG. 14 is a cross-sectional view of the reduced pressure adapter ofFIG. 13;

FIG. 15 is a bottom perspective view of a reduced pressure adapterhaving panels sensitive to the presence of microorganisms according toan exemplary embodiment of the present invention; and

FIG. 16 is a side view of the reduced pressure adapter of FIG. 15 inwhich the panels are visible through transparent or translucent sidewalls of the reduced pressure adapter.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

In the following detailed description of the preferred embodiments,reference is made to the accompanying drawings that form a part hereof,and in which is shown by way of illustration specific preferredembodiments in which the invention may be practiced. These embodimentsare described in sufficient detail to enable those skilled in the art topractice the invention, and it is understood that other embodiments maybe utilized and that logical structural, mechanical, electrical, andchemical changes may be made without departing from the spirit or scopeof the invention. To avoid detail not necessary to enable those skilledin the art to practice the invention, the description may omit certaininformation known to those skilled in the art. The following detaileddescription is, therefore, not to be taken in a limiting sense, and thescope of the present invention is defined only by the appended claims.

Reduced Pressure Adapter

Improvements in an RPWT system are disclosed that provide a reducedpressure adapter to improve the reliability of operation and prevent orreduce instances of unintentional liquid ingress into the measurementlumens of a reduced pressure delivery tube, particularly in conjunctionwith a low-profile dressing. Traditional adapters typically include botha sensing lumen and a reduced pressure delivery lumen together anelbow-shaped housing. A common cause of failure for these reducedpressure adapters results from liquid ingress into the sensing lumen,which may cause the control of therapy to become unstable and, inextreme cases, may contribute to the eventual shutdown of the device.Part of this problem is due to the location of the fluid conduction andthe nature of wound fluid in general. Wound excretions and fluids aregenerally pseudoplastic in consistency and will splash and foam in theelbow of a reduced pressure apparatus under the influence of reducedpressure. One goal of certain exemplary embodiments of the presentinvention, therefore, is to prevent the wound liquids and othernon-gaseous fluids from entering the sensing lumen.

One concept of the improved reduced pressure adapter is for the lumensto be separate down to the distribution manifold of the wound dressingso that the distribution manifold becomes the barrier between thesensing lumens and the reduced pressure path. The underside of thereduced pressure adapter is provided with channel features that attractsmall droplets splashed inside the reduced pressure adapter duringperiods of high flow or after a large slug of liquid has been pulledinto the tubing. This preferencing of the liquid and solid matter intothe larger primary lumen, and away from the smaller ancillarymeasurement lumens, helps prevent the lumens from becoming blocked. Theconcept further includes providing offset outer measurement lumen portsin the pad, which are designed such that in most orientations one of thetwo should be above the flow level in the distribution manifold of thedressing. The reduced pressure adapter is further intended to operate inconjunction with the dynamic pressure control methodologies described inmore detail below. The reduced pressure adapter may also include anadhesive drape or cover that secures the reduced pressure adapter withinthe wound. The profile of the reduced pressure adapter is low forincreased patient comfort, and the reduced pressure adapter ispreferably elbow-shaped such that the connecting tubing is routedcleanly away from the tissue site.

Reference is made first to FIG. 1 for a general description of thecomponents included in a reduced pressure wound treatment (RPWT) systemincorporating the improved elements of an exemplary embodiment of thepresent invention. The three primary components of RPWT system 10include wound dressing 12, reduced pressure delivery tube 14, and remotefluid containment and instrumentation 16.

Wound dressing 12 is generally comprised of a distribution manifold 24such as a porous pad or granular foam and a cover or drape 26 thatsecures the distribution manifold at a tissue site. Dressing 12 also mayinclude improved reduced pressure adapter 22, as shown positioned ondistribution manifold 24 and adhered thereto by an adhesive positionedon the reduced pressure adapter 22, the wound drape 26, or a separateadhesive drape associated with reduced pressure adapter 22.

Reduced pressure delivery tube 14 is a multi-lumen tube, comprised ofone or more tubing sections 28 which, as an assembled structure, providea continuous conduit between reduced pressure adapter 22 and containerconnector 34 positioned on fluid container 18. As described in moredetail below, and as known in the art, liquid and other exudates drawnby RPWT system 10 are removed from the tubing at this point and areretained within container 18. Sections of additional tubing in the formof instrumentation tubing 36 a and 36 b likewise extend from containerconnector 34 to instrumentation components 20. In certain embodiments ofthe present invention, instrumentation components 20 comprise a reducedpressure source 38 and pressure monitoring instrument components 40 aand 40 b. Described in more detail below, each of these three instrumentcomponents 20 is individually associated with one of three isolatedconduits (tubes or lumens) that extend from reduced pressure adapter 22into remote fluid containment and instrumentation 16.

Reference is now made to FIGS. 2-9 for a more detailed description ofthe reduced pressure adapter 22. FIG. 2 provides a perspective view ofthe underside of reduced pressure adapter 22 showing the variousstructural elements within the opening of reduced pressure adapter 22that are adapted to contact the distribution manifold 24 (not shown) ofthe wound dressing.

Reduced pressure adapter 22 generally comprises a base 50, which may beadhered to the distribution manifold, and a conduit housing 62 coupledto the base 50. Conduit housing 62 includes a primary conduit and a pairof ancillary conduits. The base 50 includes an aperture 53, which ispositioned over the distribution manifold and through which the liquidsand gases (collectively referred to as “fluids”) are drawn from thetissue site. A significant feature of improved reduced pressure adapter22 is the presence of channel elements positioned near and in fluidcommunication with aperture 53 and the effective way in which thechannel elements direct liquid into the primary conduit for drainage.The routing of liquids into the primary conduit maintains the ancillaryconduits of the system open for pressure measurement purposes.

Referring to FIG. 2, the conduit housing 62 of reduced pressure adapter22 includes a recessed region 54 defining an entry surface 55. Theprimary conduit terminates on the entry surface 55 at a primary port 60,which is centrally located at an apex of the recessed region 54. Theancillary conduits terminate on the entry surface 55 at ancillary ports56 and 58. The ancillary ports are positioned near diametricallyopposing edges of aperture 53.

A second end of the primary conduit terminates at a primary lumeninterface 64. Primary lumen interface 64 is generally centrallypositioned within aperture 66. Ancillary lumen interfaces 48, 49 (seeFIG. 5) to the ancillary conduits also are located within aperture 66and are described in more detail below.

FIG. 3 provides a plan view (from above) of reduced pressure adapter 22.The conduit housing 62 is preferably “elbow” shaped; however, theconduit housing may be configured at any desired angle or may extendperpendicularly from base 50. In the elbow configuration illustrated inFIG. 3, reduced pressure adapter 22 is seen to comprise base 50 and acentrally positioned conduit housing 62. Conduit housing 62 includes anelbow region 68, and the conduit housing 62 internally comprisesconduits between the ports 56, 58, 60 and the ancillary and primarylumen interfaces 48, 49, 64.

FIGS. 4, 5 & 6 show side, and end views of the reduced pressure adapter22. Reduced pressure adapter 22, as seen in the side view shown in FIG.4, is of low profile construction with base 50 defining its laterallimits. As indicated above, base 50 may be directly adhered to thedistribution manifold or may be positioned and adhered using the drapeof the wound dressing. The reduced pressure adapter 22 is positioned ondistribution manifold such that the aperture 53 (not seen in this view)of base 50 is in direct contact with the distribution manifold. In theview shown in FIG. 4, primary lumen interface 64 extends centrally outfrom conduit housing 62 and is surrounded by aperture 66. Conduitsextend through the material of reduced pressure adapter 22 between thetubing interfaces and recessed region 54, as described above. The elbowregion 68 redirects fluid flow from the wound dressing positionedbeneath reduced pressure adapter 22 to an angle associated withinterface 64 in a manner that allows the system to be placed on thewound dressing and be maintained close to the wound dressing surface.

FIG. 5 is an end view of the same structure shown in FIG. 4 with theconfiguration of elbow region 68 and the internal configuration ofconduit housing 62 more clearly shown. In this view, the same componentsassociated with adhering reduced pressure adapter 22 to the wounddressing are disclosed. Base 50 and aperture 54 are positioned asindicated in FIG. 4. Conduit housing 62 is shown as it would bepositioned to receive a section of tubing for connection to the balanceof the system of the present invention.

Internal to conduit housing 62 are primary lumen interface 64 andancillary lumen interfaces 48 and 49. Ancillary lumen interfaces 48 and49 align with the corresponding lumens in the delivery tubing by placingthe primary lumen in the tubing over the primary lumen interface 64. Thestructure of one embodiment of multi-lumen tubing used in conjunctionwith the improved reduced pressure adapter structure of the presentinvention is described in more detail below.

FIG. 6 provides essentially the same view of reduced pressure adapter 22as that of FIG. 4 but from the opposite side. Structurally, the elementsshown are the same as those shown and described with FIG. 4, which isindicative of the lateral (and to an extent, radial) symmetry of theconnector. Unless otherwise indicated, the materials used to constructthe improved connector of the present invention may be selected from anumber of materials known in the art that provide the necessaryflexibility and comfort to the patient while maintaining sufficientrigidity or resilience to maintain the open lumens that are integral tothe reduced pressure adapter function.

FIG. 7 provides a plan view (from below) of reduced pressure adapter 22and clarifies the structure and function of the various features andelements within recessed region 54 that serve to preference liquids andother non-gaseous fluids away from the ancillary ports 56, 58. In thisview, base 50 is shown surrounding the edge of recessed region 54.Ancillary ports 56 and 58 are shown positioned as indicated, withassociated conduits extending internally from ports 56 and 58 toancillary lumen interfaces (hidden and not shown in this view). Primaryport 60 can be seen centrally located within aperture 54. The primaryconduit extends (hidden and not shown in this view) from primary port 60through primary lumen interface 64. The specific structures withinrecessed region 54 that serve to conduct liquid into the primaryconduit, and thereby allow the ancillary conduits to remain unobstructedare described in more detail below with respect to FIG. 9.

FIG. 8 shows an alternate exemplary embodiment of the base associatedwith the reduced pressure adapter of the present invention. In this view(the same perspective as that of FIG. 7) added features to the undersidesurface of alternate base 52 are shown. These features, molded into thestructure of base 52, include base serrated guide channels 70, perimetercollection channels 72, and intermediate collection channels 74. Theobjective of these channels is to direct liquid away from the twoancillary measurement ports 56, 58 and into the primary port 60. Baseserrated guide channels 70 are positioned and oriented on base 50 todirectly capture and channel at least half of the liquids being drawninto the reduced pressure adapter, and indirectly channel a majorportion of the balance of the liquids being drawn in. The spaced,radially-oriented arrangement of base serrated guide channels 70 funnelsliquids away from the ancillary ports and into the primary port. Inaddition, perimeter collection channels 72 and intermediate collectionchannels 74 redirect the flow of liquids that are being drawn in betweenthe radially-oriented guide channels 70 into the guide channels 70 andaway from the ancillary ports. An example of this redirected flow isshown in FIG. 8 with bolded flow indication arrows.

Reference is now made to FIG. 9 for a more detailed description of thefeatures and elements contained within the recessed region of conduithousing 62. These features are positioned on the entry surface 55 of therecessed region 54 and are structured to preference liquids and othernon-gaseous exudates away from the ancillary ports 56, 58 and into theprimary port 60. In this view, primary port 60 is shown centrallypositioned within recessed region 54 and extending from the centrallocation to one side of recessed region 54. Ancillary ports 56 and 58are likewise disclosed in this view, positioned to either side of thecentral location of primary port 60. In this view, ancillary ports 56and 58 are circular openings (each with raised circumferential edges)that extend toward a drainage point that opens into an internal conduitextending to the associated ancillary lumen interface (not shown). Theopenings of the conduits can be seen within the confines of ancillaryports 56 and 58.

Four basic features within the structure shown in FIG. 9 are positionedto preference liquid into the primary port 60 of the reduced pressureadapter 22. The first such structure is simply the placement of theancillary ports 56 and 58 near the perimeter of the aperture 53 at alevel that is close to the surface of the distribution manifold when thereduced pressure adapter 22 is positioned thereon. In other words, whenthe reduced pressure adapter 22 is positioned on the wound dressing, theancillary ports 56 and 58 are in contact, or are nearly in contact, withthe surface of the distribution manifold. In this manner, the likelihoodof splashed or agitated liquid being directed into these ports isminimized.

The remaining three features that direct liquids into the primary portare structural serrated channels formed on various portions of the entrysurface 55 of recessed region 54. A first linear serrated channelsection 42 is positioned in association with the approximately halfcircle section of recessed region 54 that is associated with ancillaryport 58. The material that comprises the ceiling of this section ofrecessed region 54 covers and contains the conduit that extends betweenancillary port 58 and its interface (not shown). This ceiling or wall isconfigured with an array of serrated channels or striations that directsliquids that fall upon this surface towards the primary port at thecenter of the recessed region 54. Any liquids that are drawn into theopening and fall upon this portion of the entry surface 55 would bechanneled directly into primary port 60, rather than being directed intoancillary port 58.

A similar configuration is constructed in an approximately one-thirdcircular radial serrated channel section 44. Insofar as no internalconduit is contained within this section of the recessed region 54, theserrated channels in section 44 may extend deeper and more directly tothe primary port 60. These radial serrated channels are directed fromthe perimeter of aperture 54 towards the apex of the recessed region 54that drains into primary port 60. These radial striations or channelsextend from a radius adjacent ancillary port 58 radially aroundapproximately one-third of the circle to a radius adjacent ancillaryport 56. Any liquids that fall upon this portion of the recessed region54 will be directed centrally to primary port 60, rather than beingconducted to either of the ancillary ports.

Finally, the wall section that supports ancillary port 56 at the pointat which the ancillary port 56 overhangs primary port 60 is structuredwith serrated or striated channels 46 that extend downward (upward inthe normal positioning of the connector) from the opening of ancillaryport 56 towards the opening of primary port 60.

As described above, the various internal features and elements of therecessed region 54 are structured to draw liquid from most points withinthe recessed region 54 towards the centrally located primary port 60.Only liquid that enters directly into ancillary port 56 or 58 wouldlikely be drawing into an ancillary lumen. Insofar as little or nosuction is occurring at these ports, this structure greatly reduces thelikelihood of obstructions in the form of liquid or material blockagesin an ancillary lumen.

Reduced Pressure Delivery Tube

Reference is now made to FIGS. 10 and 11 for a detailed description ofthe structure of an improved reduced pressure delivery tube 80 operablein association with the system of an exemplary embodiment of the presentinvention. The reduced pressure delivery tube 80 preferably includes aprimary central lumen 82 and ancillary lumens 84 and 86. Ancillarylumens 84 and 86 are generally used for taking pressure measurements. InFIG. 11, fluid flow designated by the block arrows is shown as it wouldbe directed through primary lumen 82 while ancillary lumens 84 and 86remain generally free of liquid or any non-gaseous matter. Thecross-sectional perspectives shown in both FIGS. 10 and 11 disclose therelative cross-sectional diameters of the primary lumen 82 as comparedwith the ancillary lumens 84 and 86. Delivery device 80 has an ovalcross-section, which optimizes flexibility without allowing for thecollapse of any of the described lumens. This cross-sectional shape alsoorients the ancillary lumens 84 and 86 so that the lumens alignappropriately with the interfaces on the improved reduced pressureadapter described above.

Dynamic Method of Measuring Wound Pressure

The system of the present invention also includes an improved anddynamic method of measuring the wound pressure that overcomes problemsinherent with current reduced pressure wound treatment control systems.Various methods have been developed in the art to control the operationof reduced pressure wound treatment products and systems to insure thatthe wound pressure is maintained and that the therapy is safe byeffective operation of the prescribed regimens. Currently, woundpressure is measured with the outer lumen or lumens of a multi-lumentube that are commoned together and connected to one pressure sensor.This structure can suffer certain problems if liquid enters the lumensor they become blocked. If such liquid intrusion or blockages occur, thesystem can become unstable and alarms or indicators related to pressurebecome unreliable. Various mechanical remedies for these problems havebeen attempted and some have been partially successful. Ultimately,however, a system such as described in the prior art will be challengedwith liquid in the control lumen unless there is a physical barrierplaced against the ingress of liquid into the measurement lumen(s). Onegoal of the present invention is a system that is more reliable and morerobust when challenged with extremes of therapy, as compared to currentsingle sensor measurement lumen systems.

Reference is made to FIG. 12 wherein the system of an exemplaryembodiment of the present invention and the functional relationship ofits components are disclosed. The system incorporates two wound pressuresensors 40 a and 40 b in the system instrumentation that extendseparately (through discrete lumens or conduits) from theinstrumentation to the reduced pressure adapter and are not commoneduntil the discrete lumens combine at the interface of the reducedpressure adapter and the distribution manifold. As indicated above, thereduced pressure adapter incorporates two separate pressure sensingports as well as the fluid path through fluid chamber 18 to the reducedpressure pump 38 in the system instrumentation. Inside the systeminstrumentation, each of the ancillary measurement lumen conduits isfitted with a solenoid valve 92 and 94 which will relieve pressure tothe wound at the end of therapy, during intermittent therapy, or ifrequired to clear blockages. These valves, as well as a similar valveassociated with the reduced pressure source 38, are controlled bymicroprocessor/controller 90. Microprocessor/controller 90 likewisecontrols the operation of reduced pressure pump 38 and receives datafrom first and second pressure measurement devices 40 a and 40 b. Themicroprocessor/controller 90 is programmed to monitor the wound pressurethrough the two readings associated with the two ancillary lumen paths.In instances where liquid enters one of the lumens, the liquid willcause a delay in the pressure change response time of that lumen versusthe clear lumen. As the blockage becomes more acute so will the delay.When a delay is detected, the system will control the wound pressureaccording to that of the open lumen and will try to clear the liquidfrom the blocked lumen by opening the appropriate valve to atmosphere.The preferred programming will try to clear the blockage in this mannerseveral times. If the system is not successful in clearing the blockage,the programming will, from that point on, ignore the affected lumen andcontrol the system with the remaining clear lumen. The reduced pressureadapter design of the present invention, as described above, is such asto maximize the chances of having at least one clear ancillarymeasurement lumen at any given time.

Reduced Pressure Adapter with Rotating Function

Currently, reduced pressure adapters in RPWT systems typically allow forthe effective connection of reduced pressure wound therapy to the wound,but do not allow for the tube connection point to be repositioned (forexample, in the event that the patient is susceptible to skin breakdown)or for a situation where the user has incorrectly positioned the reducedpressure adapter (for example, in the event that the reduced pressureadapter is facing in the wrong direction). In such instances, the usermust remove and discard the reduced pressure adapter, and in someinstances the drape, which causes discomfort and is a nuisance to thepatient and user as well as an additional cost. Providing a rotation orswivel function to the reduced pressure adapter enables repositioningthe tube without having to remove and relocate the reduced pressureadapter. This ability assists in any situation where the tubing requiresrelocation to avoid tissue damage. One goal of the present invention isto provide a reduced pressure adapter structure that allows for easyrelocation of the tubing without removing and relocating the reducedpressure adapter or the wound dressing.

Reference is made to FIGS. 13 and 14 for a description of theconfiguration of an alternate preferred embodiment of the reducedpressure adapter structure. The reduced pressure adapter 110 shown inFIG. 13 employs a hard plastic inner core that forms a bearing surfaceto enable a rubber o-ring to seal against it and also to enable thebearing surface to slide past with relatively low friction. Bonded tothe hard plastic inner core is a soft thermoplastic or elastomericpolymer that acts as a protective and cushioning cover. FIGS. 13 and 14show the various circular ring components that go together to make upthe swivel connection of the present invention. A top rotating PVCcomponent 112 covers a top ABS insert ring 114 which itself issurrounded by a rubber o-ring 116. A bottom ABS insert ring 118 is shownthat holds o-ring 116 captive between it and the top ABS insert 114.Each of these rings is then fitted within the bottom PVC ring 120 whichcomes into contact with the base of the reduced pressure adapter and/orwith the wound dressing itself.

The internal features and elements associated with the reduced pressureadapter as described above in conjunction with a non-rotating embodimentare equally applicable here and may be integrated into the insidestructure of top rotating PVC component 112 by direct molding of thecomponent or by positioning a molded insert into a shell to for rotatingcomponent 112. In any event, the same benefits of the liquidpreferencing structures surrounding the lumen ports described above areobtainable with the rotating functionality of the alternate embodimentdescribed.

FIG. 14 discloses the same components mentioned above as they would beassembled and thereby shows in clearer detail the manner in which thecomponents interlock and rotate with or against each other. In thisview, the captive o-ring 116 is also shown to provide a proper seal forthe internal reduced pressure chamber formed by the reduced pressureadapter 110. In this view it is also clear how the internal features andelements in the port opening may be appropriately positioned on theunderside of top PVC component 112 to serve the function of preferencingliquid to the primary conduit as described above.

Reduced Pressure Adapter with Microorganism Indication

Current reduced pressure treatment systems do not generally alert thecaregiver to the presence of microorganisms in wound dressings. Many ofthese microorganisms can be significant factors in controlling infectionat the wound site. One goal of the present invention is to provide asystem that will alert the caregiver to significant levels of keymicroorganisms under the classification of aerobic, non-aerobic, grampositive and gram negative. The response or indication is in the form ofcolor patterns discretely reflecting the four classifications mentionedabove.

A volatile organic compound (VOC) sensitive strip mounted on the reducedpressure adapter or its associated drape is utilized in certainembodiments. When exposed to the targeted VOC known to form in thepresence of certain microorganisms, a color pattern becomes apparent andthereby identifies the type of microorganism present in the wound fluid.Referencing FIGS. 15 and 16, a reduced pressure adapter 122 includes abase 124 and a conduit housing 130 similar to that described previouslywith reference to FIGS. 2-9. The positioning of a VOC sensitive panel128 in a recessed region 126 of the conduit housing 130 is shown. InFIG. 16, it can be seen that given the translucent or transparentcharacter of the material from which the reduced pressure adapter 122 isconstructed, the VOC sensitive panel 128 can be visually inspected evenfrom the exterior while the reduced pressure adapter 122 is in placewith base 124 in position against the distribution manifold of the wounddressing. The preferable positioning of this VOC sensitive panel 128 istherefore within the recessed region 126 near the periphery of therecessed region 126 as shown. FIG. 15 shows more clearly the placementof this VOC sensitive panel within the recessed region 126 where it isconstantly exposed to the fluid materials being drawn from the wound.Alternate placements of the panels are possible as long as sufficientexposure to wound fluids exists.

It should be apparent from the foregoing that an invention havingsignificant advantages has been provided. While the invention is shownin only a few of its forms, it is not just limited but is susceptible tovarious changes and modifications without departing from the spiritthereof.

We claim:
 1. A system for providing reduced pressure to a tissue site,the system comprising: a reduced-pressure adapter; a delivery lumenfluidly coupled to the reduced-pressure adapter; a reduced-pressuresource fluidly coupled to the delivery lumen; a first measurement lumenfluidly coupled to the reduced-pressure adapter; a first pressure sensorfluidly coupled to the first measurement lumen; a first valve fluidlycoupled to the first measurement lumen; a second measurement lumenfluidly coupled to the reduced-pressure adapter; a second pressuresensor fluidly coupled to the second measurement lumen; a second valvefluidly coupled to the second measurement lumen; and a controllercoupled to the reduced-pressure source, the first pressure sensor, thefirst valve, the second pressure sensor, and the second valve, thecontroller configured to: receive data from the first pressure sensorand the second pressure sensor indicative of pressure at the tissuesite; compare data from the first pressure sensor and the secondpressure sensor, open the first valve if a response time of the firstpressure sensor is greater than a response time of the second pressuresensor; and operate the reduced-pressure source based on the data fromthe second pressure sensor if the response time of the first pressuresensor is greater than the response time of the second pressure sensor.2. The system of claim 1, wherein the reduced-pressure adaptercomprises: a base; and a housing rotatable about the base.
 3. The systemof claim 1, wherein the delivery lumen, the first measurement lumen, andthe second measurement lumen are disposed within a single tube.
 4. Thesystem of claim 3, wherein the tube has an oval cross-section.
 5. Thesystem of claim 3, wherein the delivery lumen has a diameter that islarger than a diameter of the first measurement lumen and a diameter ofthe second measurement lumen.
 6. The system of claim 1, wherein thereduced-pressure adapter comprises channels configured to direct liquidaway from the first measurement lumen and the second measurement lumen.7. The system of claim 1, further comprising: a distribution manifoldattached to the reduced-pressure adapter; and a drape comprising anadhesive surface adapted for securing the reduced-pressure adapter andthe distribution manifold to the tissue site.
 8. The system of claim 1,wherein the reduced-pressure adapter comprises: a housing having anentry surface; a primary conduit through the housing coupled to thedelivery lumen and terminating on the entry surface; a first ancillaryconduit through the housing coupled to the first measurement lumen andterminating on the entry surface; and a second ancillary conduit throughthe housing coupled to the second measurement lumen and terminating onthe entry surface.
 9. The system of claim 8, further comprising: a baseattached to the housing; and guide channels on the base.
 10. The systemof claim 8, further comprising: a base attached to the housing; andradial guide channels on the base adapted to direct liquid from aperiphery of the base away from the first ancillary conduit and thesecond ancillary conduit.
 11. A method for treating a tissue site withreduced pressure, the method comprising: providing reduced pressure tothe tissue site through a delivery lumen and a reduced-pressure adapter;receiving data indicative of pressure at the tissue site from a firstpressure sensor fluidly coupled to the tissue site by a firstmeasurement lumen and the reduced-pressure adapter and a second pressuresensor fluidly coupled to the tissue site by a second measurement lumenand the reduced-pressure adapter; comparing data from the first pressuresensor and the second pressure sensor; opening a first valve fluidlycoupled to the first measurement lumen if a response time of the firstpressure sensor is greater than a response time of the second pressuresensor; and operating a reduced-pressure source based on the data fromthe second pressure sensor if the response time of the first pressuresensor is greater than the response time of the second pressure sensor.12. The method of claim 11, wherein the reduced-pressure adaptercomprises: a base; and a housing rotatable about the base.
 13. Themethod of claim 11, wherein the delivery lumen, the first measurementlumen, and the second measurement lumen are disposed within a singletube.
 14. The method of claim 13, wherein the tube has an ovalcross-section.
 15. The method of claim 13, wherein the delivery lumenhas a diameter that is larger than a diameter of the first measurementlumen and a diameter of the second measurement lumen.
 16. The method ofclaim 11, wherein the reduced-pressure adapter comprises channelsconfigured to direct liquid away from the first measurement lumen andthe second measurement lumen.
 17. The method of claim 11, furthercomprising: a distribution manifold attached to the reduced-pressureadapter; and a drape comprising an adhesive surface adapted for securingthe reduced-pressure adapter and the distribution manifold to the tissuesite.
 18. The method of claim 11, wherein the reduced-pressure adaptercomprises: a housing having an entry surface; a primary conduit throughthe housing coupled to the delivery lumen and terminating on the entrysurface; a first ancillary conduit through the housing coupled to thefirst measurement lumen and terminating on the entry surface; and asecond ancillary conduit through the housing coupled to the secondmeasurement lumen and terminating on the entry surface.
 19. The methodof claim 18, further comprising: a base attached to the housing; andguide channels on the base.
 20. The method of claim 18, furthercomprising: a base attached to the housing; and radial guide channels onthe base adapted to direct liquid from a periphery of the base away fromthe first ancillary conduit and the second ancillary conduit.